“receptor”的搜索结果

产品 51 到 100 共 109个

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  1. Indirubin Derivative E804

    Catalog No. A21052
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    IGF1R inhibitor
    E 804 is a potent inhibitor of Insulin-like Growth Factor 1 Receptor (IGF1R), with an IC50 of 0.65 μM for IGF1R. 了解更多
  2. Loxapine

    Catalog No. A18073
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    D2DR/D4DR inhibitor
    Loxapine Succinate is a D2DR and D4DR inhibitor, serotonergic receptor antagonist and also a dibenzoxazepine anti-psychotic agent. 了解更多
  3. Resatorvid

    Catalog No. A11543
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    TLR4 inhibitor
    Resatorvid (TAK-242) is a selective Toll-like receptor 4 (TLR4) inhibitor and plays pivotal role in various inflammatory diseases. 了解更多
  4. IRAK inhibitor 4

    Catalog No. A11458
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    IRAK4 inhibitor
    IRAK inhibitor 4 is an interleukin-1 receptor associated kinase 4(IRAK4) inhibitor. 了解更多
  5. EGFR-IN-3

    Catalog No. A15847
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    EGFR inhibitor
    EGFR-IN-3 is an epidermal growth factor receptor (EGFR) inhibitor. 了解更多
  6. DDR-TRK-1

    Catalog No. A12955
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    DDR1 inhibitor
    DDR-TRK-1 is a selective Discoidin Domain Receptor 1 (DDR1) inhibitor, with an IC50 value of 9.4 nM. DDR-TRK-1 also inhibits TRK family. 了解更多
  7. RIPA-56

    Catalog No. A12473
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    RIP1 inhibitor
    RIPA-56 is a highly potent, selective, and metabolically stable inhibitor of receptor-interacting protein 1 (RIP1) with an IC50 of 13 nM. 了解更多
  8. GENZ-882706

    Catalog No. A12484
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    CSF-1R Inhibitor
    GENZ-882706 is a potent colony stimulating factor-1 receptor (CSF-1R) Inhibitor extracted from patent WO 2017015267A1. 了解更多
  9. Lestaurtinib

    Catalog No. A11274
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    multi-kinase inhibitor
    Lestaurtinib (CEP-701;KT-5555) is a multi-kinase inhibitor with potent activity against the Trk family of receptor tyrosine kinases. Lestaurtinib inhibits JAK2, FLT3 and TrkA with IC50s of 0.9, 3 and less than 25 nM, respectively. 了解更多
  10. CHMFL-EGFR-202

    Catalog No. A12524
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    EGFR inhibitor
    CHMFL-EGFR-202 is a potent, irreversible inhibitor of epidermal growth factor receptor (EGFR) mutant kinase, with IC50s of 5.3 nM and 8.3 nM for drug-resistant mutant EGFR T790M and WT EGFR kinases, respectively. 了解更多
  11. eCF506

    Catalog No. A13126
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    Src inhibitor
    eCF506 is a highly potent and orally bioavailable inhibitor of the non-receptor tyrosine kinase Src with an IC50 of less than 0.5 nM. 了解更多
  12. ALK2-IN-2

    Catalog No. A13604
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    Alk2 inhibitor
    ALK2-IN-2 is a potent and selective inhibitor of activin receptor-like kinase 2 (ALK2) with an IC50 of 9 nM, and over 700-fold selectivity against ALK3. 了解更多
  13. TD-0212

    Catalog No. A13715
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    neprilysin (NEP) inhibitor
    TD-0212 (compound 35) is an orally active dual pharmacology angiotensin II type 1 receptor (AT1) antagonist and neprilysin (NEP) inhibitor, with a pKi of 8.9 for AT1 and a pIC50 of 9.2 for NEP. 了解更多
  14. Vilazodone Hydrochloride

    Catalog No. A11604
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    serotonin transporter (SER) inhibitor
    Vilazodone Hydrochloride (EMD 68843 Hydrochloride) is a serotonin transporter (SER) inhibitor and 5-HT1A receptor partial agonist. 了解更多
  15. TRPC6-IN-1

    Catalog No. A12309
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    TRPC6 inhibitor
    TRPC6-IN-1 is a Transient Receptor Potential Canonical 6 Channel (TRPC6) inhibitor, with an EC50 of 4.66 μM. 了解更多
  16. MD2-TLR4-IN-1

    Catalog No. A18452
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    MD2-TLR4 inhibitor
    MD2-TLR4-IN-1 (compound 22m) is an inhibitor of myeloid differentiation protein 2/toll-like receptor 4 (MD2-TLR4) complex, inhibiting lipopolysaccharides (LPS)-induced expression of tumor necrosis factor alpha (TNF-α) and interleukin-6 (IL-6) in macrophages with IC50 values of 0.89 μM and 0.53 μM, respectively. 了解更多
  17. FLT3-IN-4

    Catalog No. A18509
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    FLT3 inhibitor
    FLT3-IN-4 is a potent and orally effective Fms-like tyrosine receptor kinase 3 (FLT3; IC50=7 nM) inhibitor for treating acute myelogenous leukemia. 了解更多
  18. c-Fms-IN-8

    Catalog No. A18879
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    CSF-1R, c-FMS Type II inhibitor
    c-Fms-IN-8 (compound 4a) is a colony stimulating factor-1 receptor (CSF-1R, c-FMS) Type II inhibitor, with an IC50 of 9.1 nM. 了解更多
  19. 7-BIA

    Catalog No. A18934
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    PTPRD inhibitor
    7-BIA is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with an IC50 of ~1-3 μM. 了解更多
  20. c-Fms-IN-10

    Catalog No. A19017
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    FMS inhibitor
    c-Fms-IN-10 is the derivative of thieno [3,2-d] pyrimidine, an kinase inhibitor of FMS (Colony stimulating factor-1 receptor, CSF-1R) with IC50 of 2 nM. c-Fms-IN-10 has anti-tumor activity. 了解更多
  21. LTβR-IN-1

    Catalog No. A19038
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    LTβR inhibitor
    LTβR-IN-1 is a potent, selective lymphotoxin β receptor (LTβR) inhibitor with an IC50 of 10 μM. 了解更多
  22. GSK547

    Catalog No. A19073
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    RIP1 inhibitor
    GSK547 (GSK-547) is a highly selective and potent inhibitor of receptor-interacting serine/threonine protein kinase 1 (RIP1), inhibits macrophage-mediated adaptive immune tolerance in pancreatic cancer. 了解更多
  23. GSK-843

    Catalog No. A18526
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    RIPK3 inhibitor
    GSK-843 (GSK'843) is a receptor-interacting protein kinase 3 (RIP3 or RIPK3) inhibitor, which binds RIP3 kinase domain with an IC50 of 8.6 nM, and inhibits kinase activity with an IC50 of 6.5 nM. 了解更多
  24. PK68

    Catalog No. A18582
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    RIPK1 inhibitor
    PK68 is a potent and selective type II inhibitor of receptor-interacting kinase 1 (RIPK1) with an IC50 of ~90?nM, displays inhibition of RIPK1-dependent necroptosis. 了解更多
  25. HS-1371

    Catalog No. A18653
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    RIP3 inhibitor
    HS-1371 is a potent and ATP-competitive receptor-interacting protein kinase 3 (RIP3) inhibitor with an IC50 of 20.8?nM. 了解更多
  26. TGFβRI-IN-1

    Catalog No. A18800
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    TGFβRI kinase inhibitor
    TGFβRI-IN-1 is an oral active and selective TGFβ receptor type I (TGFβRI) kinase inhibitor, with IC50 values of 2 nM and 7.6 μM for TGFβRI and TGFβRII, respectively. 了解更多
  27. WRG-28

    Catalog No. A18832
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    DDR2 inhibitor
    WRG-28 is a novel, potent and selective, allosteric inhibitor of discoidin domain receptor 2 (ddr2). 了解更多
  28. DBPR112

    Catalog No. A18857
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    EGFR 抑制剂
    DBPR112 is an orally active Furanopyrimidine-Based Epidermal Growth Factor Receptor inhibitor with IC50s of 15 nM and 48 nM for EGFRWT and EGFRL858R/T790M, respectively. 了解更多
  29. L-(-)-α-Methyldopa (hydrate)

    Catalog No. A18111
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    DOPA decarboxylase inhibitor
    Methyldopa Sesquihydrate is a DOPA decarboxylase inhibitor and indirect α2-adrenergic receptor agonist used to treat hypertension. 了解更多
  30. Molindone hydrochloride

    Catalog No. A17647
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    MAO inhibitor
    Molindone HCl is a D2 dopamine receptor antagonist. It also acts as a MAO inhibitor. 了解更多
  31. Dinoprost tromethamine

    Catalog No. A17505
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    Prostaglandin Receptor inhibitor
    Dinoprost Tromethamine, also known as Dinoprost Trometamol, is a naturally occurring prostaglandin used in medicine to induce labor and as an abortifacient. 了解更多
  32. Benorylate

    Catalog No. A17501
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    Prostaglandin Receptor inhibitor
    Benorilate, also known as Win-11450, is an ester of aspirin and paracetamol with analgesic, antipyretic, and anti-inflammatory activity used in the treatment of rheumatoid diseases. Benorilate has less severe side effects than aspirin. 了解更多
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    AG1295

    Catalog No. A17227
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    PDGFR 抑制剂
    AG1295 is a PDGF receptor specific inhibitor. 了解更多
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    BIBF0775

    Catalog No. A17230
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    TGFβRI 抑制剂
    BIBF0775 is an inhibitor of the transforming growth factor β receptor I (TGFβRI). 了解更多
  33. AX-024 hydrochloride

    Catalog No. A18332
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    TNF receptor inhibitor
    AX-024 is an orally available inhibitor of the TCR-Nck interaction that selectively inhibits TCR-triggered T cell activation (IC50 value 1 nM). Inhibiting an immediate TCR signal has promise for treating a broad spectrum of human T cell-mediated autoimmune and inflammatory diseases. 了解更多
  34. Loxapine Succinate

    Catalog No. A17347
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    D2DR and D4DR inhibitor
    Loxapine Succinate is a D2DR and D4DR inhibitor and serotonergic receptor antagonist. Loxapine succinate is an antipsychotic agent used in schizophrenia. 了解更多
  35. AG 555

    Catalog No. A18337
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    EGFR 抑制剂
    AG555 is a potent epidermal growth factor receptor (EGFR) kinase inhibitor. 了解更多
  36. Importazole

    Catalog No. A17128
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    nuclear transport receptor importin-β 抑制剂
    Importazole是Importin-β的细胞可渗透抑制剂。它可能通过改变与RanGTP的相互作用来特异性抑制importin-β的功能。 了解更多
  37. Eucalyptol

    Catalog No. A15662
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    5-HT3 receptor 抑制剂
    Eucalyptol是一种在桉树和其他植物中发现的双环单萜。它是5-HT3受体,钾通道,TNF-α的抑制剂。和IL-1β。 了解更多
  38. AX-024

    Catalog No. A16926
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    T cell receptor 抑制剂
    AX-024是一种细胞因子释放抑制剂,可以强烈抑制白介素6(IL-6),肿瘤坏死因子-α(TNFα),干扰素-γ(IFN-γ),IL-10和IL-17A的产生。 了解更多
  39. Flopropione

    Catalog No. A16550
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    5-HT1A receptor antagonist/COMT inhibitor
    Flopropione是5-HT1A受体拮抗剂,也是儿茶酚-邻甲基转移酶(COMT)抑制剂。 了解更多
  40. LY 3200882

    Catalog No. A16816
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    TGFβRI 抑制剂
    LY 3200882是有效的、高选择性TGF-β receptor type 1 (TGFβRI)抑制剂,在体外肿瘤组织和免疫细胞以及体内皮下肿瘤中,有效地以浓度依赖方式抑制TGFβ介导的SMAD磷酸化。 了解更多
  41. Antazoline HCl

    Catalog No. A16411
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    Histamine H1 receptor 抑制剂
    Antazoline HCl是第一代抗组胺药,可与组胺H1受体结合并阻断内源性组胺的作用。 了解更多
  42. YL-0919

    Catalog No. A16337
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    5-HT1A receptor 激动剂/serotonin reuptake 抑制剂
    YL0919,具有5-HT1A受体激动剂和选择性5-羟色胺再摄取抑制剂双重活性的新型抗抑郁候选药物,YL-0919抑制5-HT被大鼠大脑皮层突触小体和人重组细胞摄取的IC50值为1.78±0.34 nM和1.93±0.18 nM。 了解更多
  43. Reparixin L-lysine salt

    Catalog No. A15219
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    CXCL8 receptor 抑制剂
    Reparixin L-lysine salt是CXCL8受体的抑制剂,也抑制CXCR1和CXCR2的活化,已显示在各种损伤模型中减弱了炎症反应。 了解更多
  44. LDC1267

    Catalog No. A13003
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    TAM Receptor 抑制剂
    LDC1267是一种高选择性TAM(Tyro3,Axl和Mer)激酶抑制剂,对于Tyro3,Axl和Mer的IC50分别小于5 nM/8 nM/29 nM。 了解更多
  45. EGFR Inhibitor

    Catalog No. A13673
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    EGFR 抑制剂
    EGFR inhibitor是一种可透过细胞的4,6-二取代嘧啶化合物,可选择性抑制EGFR激酶,在体外的IC50值为21 nM,可阻断细胞中的受体自身磷酸化。 了解更多
  46. Atosiban

    Catalog No. A14334
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    peptide Oxytocin Receptor 抑制剂
    Atosiban是一种肽催产素受体抑制剂。 了解更多
  47. DDR1-IN-1

    Catalog No. A13985
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    DDR1 receptor 抑制剂
    DDR1-IN-1是一种有效的选择性DDR1受体酪氨酸激酶抑制剂,IC50/EC50为105 nM/87 nM,对DDR2的效力低4倍(IC50 = 413 nM)。 了解更多
  48. ML347

    Catalog No. A14298
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    BMP receptor 抑制剂
    ML347是一种选择性BMP受体抑制剂。 了解更多

产品 51 到 100 共 109个

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